Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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TERMINATED
50 participants
OBSERVATIONAL
Brief Summary
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Our objective is to estimate the accuracy of rotator culf tear utilizing an ultrasound.
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Detailed Description
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Conditions
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Study Design
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CASE_CROSSOVER
CROSS_SECTIONAL
Study Groups
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1
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Size of the tear till 2.5 cm
* The opposite tendon-normal
Exclusion Criteria
* Injury to the shoulder after the previous US.
* Pregnancy
35 Years
65 Years
ALL
No
Sponsors
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Hadassah Medical Organization
OTHER
Responsible Party
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Hadassah Medical Organization
Principal Investigators
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Ori Safran, MD
Role: PRINCIPAL_INVESTIGATOR
Hadassah Medical Organization
Locations
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Hadassah Orthopedic Department
Jerusalem, , Israel
Countries
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Other Identifiers
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SAF02-HMO-CTIL
Identifier Type: -
Identifier Source: org_study_id
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